Human Phenotype Ontology

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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Grandparent Node:
Abnormal placental membrane morphology (HP:0011409)

Parent Node:
Abnormality of the upper limb (HP:0002817)

Parent Node:
Amniotic constriction ring (HP:0009775)

..Starting node
..Amniotic constriction rings of arms (HP:0010483)

Term ID:

10483

Name:

Amniotic constriction rings of arms

Synonym:

Definition:

Amniotic constriction rings affecting the arms.

Comments:

Reference:

HP:0010483

Genes and Diseases:

Child Nodes:

Sister Nodes:

Amniotic constriction rings of legs (HP:0010495)

Digital constriction ring (HP:0010491)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0010483	HP:0010483	Amniotic constriction rings of arms	0	CL E G H

Genes (0) :

Diseases (0) :

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.